Canonical Allele Identifier: CA2008250919

Gene: KCNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839713C= , CM000673.2:g.128839713C=	GRCh38
NC_000011.9:g.128709608C= , CM000673.1:g.128709608C=	GRCh37
NC_000011.8:g.128214818C=	NCBI36
NG_009379.1:g.32661G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.531G= MANE Select	ENSP00000376434.1:p.Lys177=
ENST00000324036.7:c.531G=	ENSP00000316233.3:p.Lys177=
ENST00000392664.2:c.588G=	ENSP00000376432.2:p.Lys196=
ENST00000392665.6:c.531G=	ENSP00000376433.2:p.Lys177=
ENST00000392666.5:c.531G=	ENSP00000376434.1:p.Lys177=
ENST00000440599.6:c.531G=	ENSP00000406320.2:p.Lys177=
NM_000220.4:c.588G=	NP_000211.1:p.Lys196=
NM_153764.2:c.531G=	NP_722448.1:p.Lys177=
NM_153765.2:c.582G=	NP_722449.3:p.Lys194=
NM_153766.2:c.531G=	NP_722450.1:p.Lys177=
NM_153767.3:c.531G=	NP_722451.1:p.Lys177=
NM_000220.6:c.588G=	NP_000211.1:p.Lys196=
NM_153764.3:c.531G=	NP_722448.1:p.Lys177=
NM_153765.3:c.582G=	NP_722449.3:p.Lys194=
NM_153766.3:c.531G= MANE Select	NP_722450.1:p.Lys177=
NM_153767.4:c.531G=	NP_722451.1:p.Lys177=